{"id":406,"date":"2018-12-03T04:23:25","date_gmt":"2018-12-03T04:23:25","guid":{"rendered":"http:\/\/www.gyanvihar.org\/journals\/?p=406"},"modified":"2019-06-12T05:46:45","modified_gmt":"2019-06-12T05:46:45","slug":"enantiomeric-separation-of-betaxolol-using-liquid-chromatographic-techniques-a-review","status":"publish","type":"post","link":"https:\/\/www.gyanvihar.org\/journals\/enantiomeric-separation-of-betaxolol-using-liquid-chromatographic-techniques-a-review\/","title":{"rendered":"Enantiomeric separation of betaxolol using liquid chromatographic techniques: A review"},"content":{"rendered":"

pp<\/strong>. 35-41<\/strong><\/span><\/p>\n

H<\/strong>ariom Nagar<\/strong><\/span><\/p>\n

Suresh Gyan Vihar University, Jaipur-302017, Rajasthan, India.<\/em><\/span><\/p>\n

Email: hariomnagariitr@gmail.com, <\/a>hariom.nagar@mygyanvihar<\/u><\/span><\/p>\n

ABSTRACT: <\/strong>Amino alcohols like \u03b2-blockers are very important drugs for the treatment of heart related diseases. This is due to presence of active functional groups (-OH and NH2) in their unique and simple structure. Betaxolol a selective \u03b21-receptor antagonist is one of the most prescribed drug for treatment of particularly hypertension, and it is also a very strong antiglaucoma agent. (S)-(\u2212)-enantiomer of \u03b2-blockers shows about 50-500 fold higher pharmacological activities, due to the specific and proper orientation of groups to react with \u03b21- receptor. There has been no attempt to review on the enantiomeric separation of betaxolol using chromatographic techniques. This paper deals with the application of: high-performance liquid chromatography by direct method, using chiral stationary phases and, by indirect method using chiral derivatizing reagent and; thin layer chromatography by direct method using chiral selector as chiral impregnating reagent, chiral inducing reagent and chiral mobile phase additives.<\/span><\/p>\n

Keywords: <\/strong>\u03b2-blockers, chiral selector, enantiomeric separation, thin layer chromatography, high-performance liquid chromatography, chiral derivatizing reagent<\/span><\/p>\n

INTRODUCTION<\/span><\/h2>\n

\u03b2-blockers (also known as \u03b2-adrenolytic drugs) consist of a group of synthetic chiral hydroxyl \u00a0amine-containing \u00a0compounds \u00a0with pKa \u223c 9.2. They stop adrenaline from binding to \u00a0nerve \u00a0receptors \u00a0and \u00a0\u201cblock\u201d \u00a0its \u00a0effects. Betaxolol a potent \u03b21- receptor blocker used in the treatment of hypertension and glaucoma. It shows greater af\ufb01nity for \u03b21-receptor than metoprolol. The (S)-( \u0336 )-enantiomer of betaxolol drug (Figure<\/strong>) is pharmacologically effective, showing about 50\u2013500-fold higher activities (Lee and William 1990). In most cases betaxolol is administered as racemic mixtures. Since the enantiomers have different activity in \u2018chiral environment of our body\u2019 therefore these enantiomers are considered different compounds. Many biologists and clinical pharmacologists tend to deal with enantiomeric\u00a0\u00a0 \u00a0mixtures\u00a0\u00a0\u00a0\u00a0 of\u00a0\u00a0\u00a0 \u00a0isomers.\u00a0\u00a0\u00a0\u00a0 A physician, presenting such a drug under a brand name is unaware of different activity of enantiomers and may make mistakes (Ariens 1984). Therefore, many regulatory agencies ask the pharmacologists to present full pharmacokinetics and pharmacological information of both the enantiomers. Because in certain cases, the less reactive or unwanted enantiomer can have side effects or even toxic effects. Therefore,\u00a0 efficient methods\u00a0 of enantioresolution are always required to control the enantiomeric purity or to resolve racemic mixtures and to determine optical purity of the drugs.<\/span><\/p>\n

Enantiomeric separation has immense importance in various fields from academic and industrial point\u00a0 of view. For enantiomeric separation two basic strategies \u2018\u2018direct approach<\/em>\u2019\u2019 and \u2018\u2018indirect approach<\/em>\u2019\u2019 have evolved in recent years. The direct approach has no require derivatization and separation can be achieved by using chiral selector: as chiral impregnating reagent, chiral mobile phase additives and chiral inducing reagent in thin layer chromatography and; as chiral stationary phase in high-performance liquid chromatography, to produce chiral environment in situ <\/em>formation of transient diastereomers between enantiomers present in analyte and the enantiomer of pure chiral selector. In indirect method, there is first conversion of the enantiomers of analyte species in to daistereomers by reacting them with chiral derivatizing reagents and then separation can be done by chromatography in achiral environment.<\/span><\/p>\n

In literature review there have been reported some \u00a0basic \u00a0approaches \u00a0and \u00a0principles \u00a0of planar and column chromatography for enantiomeric separation\u00a0 of\u00a0 betaxolol. Nevertheless, there has been no attempt to review on the enantiomeric separation of betaxolol by chromatography using the direct and indirect approaches. The present paper focused on the use of liquid chromatography for the enantiomeric separation of betaxolol.<\/span><\/p>\n

DIRECT APPROACH<\/span><\/h1>\n

Ennatiomeric separation using direct approach is depends on the chiral environment which is either produced by incorporating a suitable chiral selector at an appropriate stage or created in the form of chiral stationary phase (CSP). This chiral invironment can be created in thin-layer chromatography (TLC) and high- performance liquid chromatography (HPLC) by (a) preparing the TLC plate or the column with the chiral selector, (b) impregnating the chiral selector on stationary phase of TLC, or (c) adding the chiral selector to the mobile phase. The material mentioned at (a) is chiral owing to its own structure (e.g. cellulose) while the material mentioned at (b) is prepared by bonding the chiral selector of interest to reactive groups of inert support. \u00a0In situation\u00a0<\/span>(c) chiral environment is created by mixing the chiral\u00a0 selector\u00a0 and with mobile\u00a0 phase and flow of this mixture prior to separation. In all the cases, transient daistereomers are formed on the surface by the interaction of chiral selector with enantiomers of analyte of interest. The separation of these enantiomers is based on the concept is that, the\u00a0\u00a0 \u00a0enantiomer\u00a0\u00a0 \u00a0forming\u00a0\u00a0 \u00a0most\u00a0\u00a0 \u00a0stable\u00a0<\/span>daistereomers will be most retained with stationary phase it means elute later and the enantiomer forming less stable daistereomer elute earlier. Martens and Bhushan (1990) direct methods for separation of enentiomers are important in various fields like synthetic and mechanistic study, pharmaceutuical and biomedical analysis.<\/span><\/p>\n

Enantiomeric separation by TLC<\/span><\/h1>\n

Using Impregnation<\/span><\/h2>\n

The technique in which a suitable chiral selector is incorporating with the adsorbent without covalently affecting its inert character, owing to application of samples on the plate for their separation is termed as impregnated TLC. There are various methods used for impregnation of TLC: spraying the solution of the impregnating reagent on the plate; immersing plain plate or ascending or descending the plate in a normal manner of development into an appropriate solution of the impregnating reagent; exposing the thin layer to the vapors of the impregnating reagent; and mixing the chiral selector with the inert support. In case of immersion there may be peeling of the thin layer, and in spraying method less uniform dispersion of the chiral selector on inert support than in the mixing of chiral selector with inert support or immersion (Bhushan and Martens, 1997).<\/span><\/p>\n

The overall results of resolution are depends on the kind of the functional groups and chemical nature of the impregnating reagent the compounds being separated, along with the influence of the impregnating\u00a0<\/span>reagent on the partition\/or adsorption. The methods used for impregnation also play important role in the resolution of the enantiomers.<\/span><\/p>\n

This method provides an inexpensive and wide choice of chromatographic conditions for enantiomeric separation of variety of compounds. Enantiomeric separation of betaxolol has been carried out using the L-lysine\/L-arginine (Bhushan and Thiong\u2019O, 1998), as chiral impregnating reagent and chromatographic data in terms of resolution and limit of detection (LOD) are given in Table<\/strong>.<\/span><\/p>\n

Using chiral inducing reagent (CIR)<\/span><\/h2>\n

CIR: The chiral selector when mixed with the racemic mixture of the analyte then itself induced the chiral environment in medium prior to formation of transient daistereomers of analyte, so it is called the chiral inducing reagent. The advantages of this method over the impregnation is that the required quantity of the chiral selector is very less than the quantity of the chiral selctor required in impregnation methods. Since, in this method no requirement to produce chiral environment on the inert support of TLC for separation of enantiomers. Therefore, the TLC is called as achiral TLC and the separation is known as achiral phase chromatographic separation.<\/span><\/p>\n

Literature reported the use of (S)- Glutamic acid as CIR and chromatographic run was performed, results obtained were good in terms of RS <\/em>(Bhushan et al. 2015).<\/span><\/p>\n

Enantiomeric separation by HPLC<\/span><\/h1>\n

It is most widely used method for the enantiomeric separation. Several chiral columns have been used in recent years for enantiomeric separation. These chiral column are commercially available in market. This method gives better result than the TLC method in regard of accuracy, precision and detection limit of the analyte. The detectors generally used in this technique is photodiode array detector (PDA) 2600, make the detection of analyte molecules up to pico meter level. Several columns containing chiral stationary phases, based\u00a0\u00a0 \u00a0on:\u00a0\u00a0 \u00a0cellulose,\u00a0\u00a0 \u00a0amylose,\u00a0\u00a0 \u00a0pirkle,\u00a0<\/span>used for enantioseparation.\u00a0<\/span>Of the above stationary phase based columns, certain have been used for enantioseparation of betaxolol; Cellulose tris(3,5-dichlorophenyl-carbamate) (Ates et al. 2013), Cellulose tris(3,5-dimethylphenyl- carbamate), (Peng et al, <\/em>2010), Amylose tris(3,5-dimethoxyphenyl carbamate), (Cass et al. 1999), and comparative data in terms of resolution time, limit of detection and resolution values, are given in Table.<\/strong><\/span><\/p>\n

INDIRECT \u00a0APPROACH<\/span><\/h1>\n

Chromatographic conditions of indirect method can be optimized more easily than the direct method, therefore, separation of daistereomeric pair via indirect method is sometimes simpler and often better resolution obtained. High sensitive detector response in this technique is providing better determination of biological samples in blood and urine. The CDR used for derivatization of samples are generally chosen with good\u00a0<\/span>limit of detection. For example the Marfey\u2019s based CDRs shows high sensitive detector response to samples because of high molar UV-Vis absorptivity (\u025b) and fluorescence quantum yield. The reaction of CDR react with enantiomers of (\u00b1)- or the (R,S<\/em>)-mixture is of different rates, therefore derivatization conditions must be optimized.\u00a0<\/span>In the structure of analyte sample suitable reactive group should be in close proximity to the stereogenic center, which is prone a quantitative transformation with the CDR and without forming the side products. Racemization must not be there of the sample and of the CDR in the reaction, which transforms the enantiomeric mixture into daistereomers.<\/span><\/p>\n

Enantiomers \u00a0of \u00a0betaxolol \u00a0has \u00a0been separated\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 by\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 converting\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 them\u00a0\u00a0\u00a0 into daistereomers. \u00a0Several \u00a0CDRs \u00a0have \u00a0been used for the formation of daistereomers of betaxolol prior to their separation by HPLC. In Table <\/strong>separation data are given in terms of\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 \u2018\u2018resolution\u2019\u2019\u00a0\u00a0 of\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 daistereomers\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 of betaxolol formed with following CDRs: (\u2013)- (\u03b1-methoxy-(\u03b1- (trifluoromethyl)phenylacetyl chloride (Kim et\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 al.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2001);\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 1,3-diacetoxy-1-(4-nitro- phenyl)-2-propyl isothiocyanate (P\u00e9ter and F\u00fcl\u00f6p,\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2001);\u00a0 2,3,4,6-tetra-O-acetyl-b-D- galactopyranosyl\u00a0 isothiocyanate \u00a0(Ko\u00a0 et \u00a0al. 2006);\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2,3,4,6-tetra-O-acetyl-b-D- glucopyranosyl \u00a0isothiocyanate \u00a0(Ko \u00a0et \u00a0al. 2006). Marfey\u2019s reagent based CDRs; \u00a0(R)- 2-(5-\ufb02uoro-2,4-dinitrophenylamino)-3- (methylthio)propanoic\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 acid,\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (S)-N-(1- cyclohexylethyl)-5-\ufb02uoro-2,4- dinitrobenzenamine,\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (R)-5-\ufb02uoro-2,4- dinitro-n-(1-phenylethyl)benzenamine, have\u00a0<\/span>been used by Bhushan and Nagar (2014) for synthesis of daistereomers of betaxolol and the structures of these daistereomers also optimized by using 09 Rev A. 02 and hybrid density functional B3LYP with 6-31G basis set.<\/span><\/p>\n

CONCLUSIONS<\/span><\/h1>\n

The liquid chromatography using direct and indirect methods are very useful for quantitative and qualitative analysis of important pharmaceuticals. Direct method is more suitable for separation of enantiomers in their pure form without any derivatization and is less time consuming. Direct TLC method (i) is less expensive in comparison to HPLC, GC and capillary electrophoresis that require highly expensive experimental set-up and running costs, (ii) is successful for rapid and sensitive resolution, detection and isolation of enantiomers in a range lower than the limits prescribed (1%) for pharmaceuticals in industry. Direct HPLC is widely used method for separation of enantiomers because (i) most of the CSPs are commercially available in market, (ii) detection and isolation limit is up to pico meter level, (iii) no requirement of derivatization hence less time consuming. But the chiral column is of high cost in direct method, while in indirect method no requirement of chiral column so indirect HPLC is less expensive and therefore more useful for detection of enantiomers.<\/span><\/p>\n

ACKNOWLEDGEMENT<\/span><\/h1>\n

The author (H Nagar) is grateful to SGVU, Jaipur for providing the technical facilities and peaceful environment for doing this job.<\/span><\/p>\n

REFERENCES<\/span><\/h1>\n

Lee, \u00a0E.J.\u00a0\u00a0\u00a0 and\u00a0 William,\u00a0 K.M.\u00a0 (1990).\u00a0<\/span>Chirality: Clinical pharmacokinetic and pharmacodynamic considerations. Clin. Pharmacokinet. <\/em>18: 339\u2013345.<\/span><\/p>\n

Ari\u00ebns, E.J. (1984). Stereochemistry, a basis for sophisticated nonsense in pharmacokinetics and clinical pharmacology. Eur. J. Clin. Pharmacol. <\/em>26: 663\u2013668.<\/span><\/p>\n

Bhushan, R. and Thiong\u2019O, G.T. (1998).\u00a0<\/span>Direct enantioseparation of some \u03b2- adrenergic blocking agents using impregnated thin-layer chromatography. J. Chromatogr. B <\/em>708: 330-334.<\/span><\/p>\n

Bhushan, \u00a0R. \u00a0and \u00a0Martens, \u00a0J. \u00a0(1997).\u00a0<\/span>Direct resolution of enantiomers of impregnated TLC. Biomed. Chromatogr. <\/em>11: 280-285.<\/span><\/p>\n

Bhushan, R., Nagar, H. and Martens, J. (2015). Resolution of enantiomers with both achiral phases in chromatography: conceptual challenge.\u00a0 \u00a0RSC\u00a0 \u00a0Adv.\u00a0 \u00a0<\/em>5:\u00a0 \u00a028316-\u00a0<\/span>28323.<\/span><\/p>\n

Ates, H., Younes, A.A., Mangelings, D., and Heyden, Y.V. (2013). Enantioselectivity of polysaccharide- based chiral selectors in polar organic solvents chromatography: Implementation of chlorinated selectors in a separation strategy. J. Chromatogr. Biomed. <\/em>74: 1\u201313.<\/span><\/p>\n

Peng, L., Jayapalan, S., Chankvetadze, B., and Farkas, T. (2010). Reversed- phase chiral HPLC and LC-MS analysis with\u00a0<\/span>tris(chloromethylphenylcarbamate) derivatives of cellulose and amylose as\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 chiral\u00a0\u00a0 stationary\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 phases.\u00a0 J.<\/em> Chromatogr. A <\/em>1217: 6942\u20136955.<\/span><\/p>\n

Cass, Q.B., Tiritan, M.E., Calafatti, S.A.,\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0Matlin,\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0S.A.\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0(1999).\u00a0<\/span>Enantioseparation on amylose tris (3, 5-dimethoxyphenyl carbamate): application to commercial pharmaceutical chiral drugs. J. Liq. Chromatogr. Rel. Technol. <\/em>22 3091\u2013<\/span>3099.<\/span><\/p>\n

Kim, K.H., Lee, J.H., Ko, M.Y., Hong,\u00a0<\/span>S.P. and Youm, J.R. (2001). Chiral separation of \u03b2-blockers after derivatization with (\u2013)-a-Methoxy-a- (tri\ufb02uoromethyl)phenylacetyl\u00a0<\/span>chloride\u00a0 \u00a0by\u00a0 \u00a0gas\u00a0 \u00a0chromatography.<\/span><\/p>\n

Arch. Pharm. Res. <\/em>24: 402\u2013406. p<\/span>\u00e9ter,\u00a0\u00a0\u00a0 M.\u00a0\u00a0\u00a0 and\u00a0\u00a0\u00a0 F\u00fcl\u00f6p,\u00a0\u00a0\u00a0 F.\u00a0\u00a0\u00a0 (2002).\u00a0<\/span>Comparison of isothiocyanate chiral derivatizing reagents for highnperformance liquid chromatography. Chromatographia <\/em>56: 631\u2013636.<\/span><\/p>\n

Ko,\u00a0\u00a0\u00a0 M.Y.,\u00a0\u00a0\u00a0 Shin,\u00a0\u00a0\u00a0 D.H.,\u00a0\u00a0\u00a0 Oh,\u00a0\u00a0\u00a0 J.W.,\u00a0<\/span>Asegahegn, W.S. and Kim, K.H. (2006). Chiral separation of \u03b2<\/em>nblockers after derivatization with a new chiral derivatization agent, GATC. Arch. Pharm. Res. <\/em>29: 1061\u2013<\/span>1065.<\/span><\/p>\n

Bhushan, R. and Nagar, H., Enantioseparation of orciprenaline, betaxolol, and propranolol using HPLC and new chiral reagents based on\u00a0\u00a0\u00a0\u00a0 1,5-difluoro-2,4-dinitrobenzene. Anal. Lett. <\/em>29 (2014) 202-219.<\/span><\/p>\n

Figure<\/span><\/h2>\n

\"\"<\/p>\n

Table\u00a0\u00a0 <\/strong>Literature reports with present study on chromatographic separation (in terms of: R<\/em>S, LOD and resolution time) of enantiomers of Bel using different CSPs\/chiral selectors\/CDRs\/CIR<\/span><\/p>\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n\n
S.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 CSPa\/CDRc\/Chiral Selectorb\/CIRd\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Technique\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Resolution time\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 LOD\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 R<\/em>S\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Reference<\/p>\n

No.\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 used\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (tR\/k\/run time)<\/td>\n<\/tr>\n

5\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Cellulose tris(3,5-dichlorophenyl-\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 i\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 0.81\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 23<\/p>\n

carbamate) a<\/td>\n<\/tr>\n

6\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Cellulose tris(3,5-dimethylphenyl-\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 i\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 15.2\/16.9 min \u00a0(tR1\/tR2)\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 1.6\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 24<\/p>\n

carbamate) a<\/td>\n<\/tr>\n

7\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Amylose tris(3,5-dimethoxyphenyl\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 i\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 11.8\/14.8 min (tR1\/tR2)\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 10 \u00b5g\/mL\u00a0\u00a0\u00a0\u00a0\u00a0 1.54\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 25<\/p>\n

8\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 carbamate) a\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 31.7\/32.9 (tR1\/tR2)\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 26<\/td>\n<\/tr>\n

(\u2013)-(\u03b1<\/em>-methoxy-(\u03b1<\/em>-(trifluoro-\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 ii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 19.8\/20.0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 1.18\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Kim 2001)<\/p>\n

9\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 methyl)phenylacetyl chlorideb\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (k<\/em>1\/k<\/em>2)<\/td>\n<\/tr>\n

1,3-diacetoxy-1-(4-nitro-phenyl)-2-propyl\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 4.67\/5.58 (k<\/em>1\/k<\/em>2)\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 0.2nmol\/\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 1.62<\/p>\n

10\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 isothiocyanateb\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 mL\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 P\u00e9ter,<\/p>\n

ii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2001<\/td>\n<\/tr>\n

2,3,4,6-tetra-O-acetyl-b-D-galactopyranosyl\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 ii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 6.32\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (Ko, et al, isothiocyanateb\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2006)<\/td>\n<\/tr>\n
2,3,4,6-tetra-O-acetyl-b-D-glucopyranosyl\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 ii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 4.70\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (Ko, et al,<\/p>\n

13\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 isothiocyanateb\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2006)<\/td>\n<\/tr>\n

14\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (R)-2-(5-\ufb02uoro-2,4-dinitrophenylamino)-3-\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 ii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 21.48\/23.88 (tR1\/tR2)\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 12pgmL-1\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 11.72\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (Bhushan<\/p>\n

(methylthio)propanoic acidb\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 and\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 and Nagar\u00a013pgmL-1\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2014)<\/td>\n<\/tr>\n

(S)-N-(1-cyclohexylethyl)-5-\ufb02uoro-2,4-\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 ii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 34.71\/36.92 (tR1\/tR2)\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 12pgmL-1\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 9.65\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (Bhushan<\/p>\n

dinitrobenzenamineb\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 and\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 and Nagar<\/p>\n

13pgmL-1\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2014)<\/td>\n<\/tr>\n

(R)-5-\ufb02uoro-2,4-dinitro-n-(1-\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 ii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 33.64\/35.63 (tR1\/tR2)\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 12pgmL-1\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 8.70\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (Bhushan<\/p>\n

phenylethyl)benzenamineb\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 and\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 and Nagar<\/p>\n

13pgmL-1\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2014)<\/td>\n<\/tr>\n

L-lysine\/L-argininec\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 5.50\/6.45 (k<\/em>1\/k<\/em>2)\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 NA\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 2.0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 Bhushan<\/p>\n

14\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 and<\/p>\n

Thiong\u2019O,<\/p>\n

iii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 1998<\/td>\n<\/tr>\n

18\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 iii\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 1.2-1.8 \u00b5g\u00a0\u00a0\u00a0\u00a0\u00a0 2.0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 (Bhushan L-Glutamic acid d\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 \u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 10 min (run time)\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0\u00a0 et al.<\/p>\n

2015)<\/td>\n<\/tr>\n

CSP, chiral stationary phase; CDR, chiral derivatizing reagent; CIR, chiral inducing reagent; tR1 and tR2 are the retention time of first and second eluting isomer, respectively; k1 and k2, retention factor of first eluting isomer; run time, time taken by solvent system to migrate across the TLC plate. i, ii and iii represent the techniques used as direct HPLC, indirect HPLC and direct TLC separation, respectively.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n

\n","protected":false},"excerpt":{"rendered":"

pp. 35-41 Hariom Nagar Suresh Gyan Vihar University, Jaipur-302017, Rajasthan, India. Email: hariomnagariitr@gmail.com, hariom.nagar@mygyanvihar ABSTRACT: Amino alcohols like \u03b2-blockers are very important drugs for the treatment of heart related diseases. This is due to presence of active functional groups (-OH and NH2) in their unique and simple structure. Betaxolol a selective \u03b21-receptor antagonist is one […]<\/p>\n","protected":false},"author":3,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[18,44],"tags":[],"class_list":["post-406","post","type-post","status-publish","format-standard","hentry","category-journal-of-environment-science-and-technology","category-volume-3-issue-2-2017-journal-of-environment-science-and-technology"],"yoast_head":"\nresearch journal - Research Journal<\/title>\n<meta name=\"description\" content=\"Amino alcohols like \u03b2-blockers are very important drugs for the treatment of heart related diseases. Research paper available at SGVU. 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